EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
01 1Ferring Korea Co., Ltd.
01 1Dinoprostone
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Ferring Korea Co., Ltd.
Registration Date : 2022-11-02
Registration Number : 20221102-209-J-1396
Manufacturer Name : EUROAPI Hungary Ltd.
Manufacturer Address : To u. 1-5., Budapest, 1045, Hungary
40
PharmaCompass offers a list of Dinoprostone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dinoprostone manufacturer or Dinoprostone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprostone manufacturer or Dinoprostone supplier.
A Cervidil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cervidil, including repackagers and relabelers. The FDA regulates Cervidil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cervidil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cervidil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cervidil supplier is an individual or a company that provides Cervidil active pharmaceutical ingredient (API) or Cervidil finished formulations upon request. The Cervidil suppliers may include Cervidil API manufacturers, exporters, distributors and traders.
click here to find a list of Cervidil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Cervidil Drug Master File in Korea (Cervidil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cervidil. The MFDS reviews the Cervidil KDMF as part of the drug registration process and uses the information provided in the Cervidil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cervidil KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Cervidil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cervidil suppliers with KDMF on PharmaCompass.
